Linked Data
COSMIC:
COSM4914017
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121137432C>A , CM000673.2:g.121137432C>A | GRCh38 |
| NC_000011.9:g.121008141C>A , CM000673.1:g.121008141C>A | GRCh37 |
| NC_000011.8:g.120513351C>A | NCBI36 |
| NG_011633.1:g.39767C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392793.6:c.2953C>A (TECTA) MANE Select | ENSP00000376543.1:p.Pro985Thr | |
| ENST00000642222.1:c.2953C>A (TECTA) | ENSP00000493855.1:p.Pro985Thr | |
| ENST00000645008.1:c.260C>A (TECTA) | ||
| ENST00000264037.2:c.2953C>A (TECTA) | ENSP00000264037.2:p.Pro985Thr | |
| ENST00000392793.5:c.2953C>A (TECTA) | ENSP00000376543.1:p.Pro985Thr | |
| NM_005422.2:c.2953C>A (TECTA) | NP_005413.2:p.Pro985Thr | |
| NM_001378761.1:c.3910C>A (TBCEL-TECTA) | NP_001365690.1:p.Pro1304Thr | |
| NM_005422.4:c.2953C>A (TECTA) MANE Select | NP_005413.2:p.Pro985Thr |